HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 479097Generated: October 26, 2026
Piperazine → 3-Piperazin-1-ylmethyl-pyrimido[5,4-e][1,2,4]triazine-5,7-diamine
https://huagongshe.com/reaction/479097
Participants
| Role | Name | HCID | Charge |
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| Reactant | Piperazine | HCID 4837 | — |
| Reactant | HCID 11390207 | HCID 11390207 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-Piperazin-1-ylmethyl-pyrimido[5,4-e][1,2,4]triazine-5,7-diamine | HCID 12109536 | 58% |
Reaction Steps
A mixture of 3-Chloromethyl-pyrimido[5,4-e][1,2,4]triazine-5,7-diamine 3 (2.00 g; 9.5 mmol) and piperazine (2.50 g; 29 mmol) in absolute ethanol was heated to 100° C. in a sealed tube for 4 h. The mixture was then allowed to cool to room temperature and evaporated. The crude product was purified by reverse phase HPLC (Rainin C18, 0% CH3CN to 30% CH3CN gradient, CH3CN/H2O, 0.1% TFA) and the bright yellow fractions containing the product were lyophilized after removal of CH3CN in vacuo to give 1.44 g of yellow colored 3-Piperazin-1-ylmethyl-pyrimido[5,4-e][1,2,4]triazine-5,7-diamine 5 as the trifluoroacetate salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06642381B2 |
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| Source dataset | uspto-grants-2003_11 |
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| ORD ID | ord-cc7eec651525458d97a73fc51172fa12 |
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| Source note | uspto-grants-2003_11 |
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